Dongyi Han

3.0k citations

128 papers · 1.8k · h-index 22

Impact in

Sensory Systems top 0.2%
- Hearing, Cochlea, Tinnitus, Genetics
Otorhinolaryngology top 1%
- Ear Surgery and Otitis Media

Papers in

Sensory Systems 68
- Hearing, Cochlea, Tinnitus, Genetics 68
Molecular Biology 29
- Mitochondrial Function and Pathology 15
- RNA and protein synthesis mechanisms 8
- Connexins and lens biology 7

Co-authors: Pu Dai (59 shared papers)Huijun Yuan (34 shared papers)Min‐Xin Guan (11 shared papers)Yongyi Yuan (19 shared papers)Dongyang Kang (26 shared papers)Deliang Huang (25 shared papers)Ronghua Li (4 shared papers)Qiuju Wang (9 shared papers)
Journals: Acta Oto-Laryngologica (19 papers)Journal of Translational Medicine (7 papers)PLoS ONE (6 papers)Biochemical and Biophysical Research Communications (6 papers)European Archives of Oto-Rhino-Laryngology (3 papers)
Partner nations: China United States Philippines

In The Last Decade

Dongyi Han

121 papers receiving 1.8k citations

Peers

Countries citing papers authored by Dongyi Han

Since Specialization

Citations

This map shows the geographic impact of Dongyi Han's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Dongyi Han with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dongyi Han more than expected).

Fields of papers citing papers by Dongyi Han

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dongyi Han. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Dongyi Han. The network helps show where Dongyi Han may publish in the future.

Co-authors

The 25 scholars most cited alongside Dongyi Han, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Dongyi Han Line = papers co-authored together Dongyi Han links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 128 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family The American Journal of Human Genetics ·Hui Zhao, Ronghua Li, Qiuju Wang, Qingfeng Yan, Jian-Hong Deng, Dongyi Han, Yidong Bai, Wie-Yen Young, Min‐Xin Guan	2004	286
2	Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China Journal of Translational Medicine ·Yongyi Yuan, Yiwen You, Deliang Huang, Jinghong Cui, Yong Wang, Qiang Wang, Fei Yu, Dongyang Kang, Huijun Yuan, Dongyi Han, Pu Dai	2009	131
3	Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA^Ser(UCN) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside‐induced and nonsyndromic hearing loss American Journal of Medical Genetics Part A ·Huijun Yuan, Yaping Qian, Yanjun Xu, Juyang Cao, Linna Bai, Weidong Shen, Fei Ji, Xin Zhang, Dongyang Kang, Jun Qin Mo, John H. Greinwald, Dongyi Han, Suoqiang Zhai, Wie‐Yen Young, Min‐Xin Guan	2005	72
4	The prevalence of the 235delC GJB2 mutation in a Chinese deaf population Genetics in Medicine ·Pu Dai, Fei Yu, Bing Han, Yongyi Yuan, Qi Li, Guojian Wang, Xin Liu, Jia He, Deliang Huang, Dongyang Kang, Xin Zhang, Huijun Yuan, Eric Schmitt, Dongyi Han, Lee‐Jun C. Wong	2007	65
5	Variants in mitochondrial tRNA^Glu, tRNA^Arg, and tRNA^Thr may influence the phenotypic manifestation of deafness‐associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss American Journal of Medical Genetics Part A ·Wie‐Yen Young, Lidong Zhao, Yaping Qian, Ronghua Li, Jing Chen, Huijun Yuan, Pu Dai, Suoqiang Zhai, Dongyi Han, Min‐Xin Guan	2006	60
6	SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss Genetics in Medicine ·Pu Dai, Qi Li, Deliang Huang, Yongyi Yuan, Dongyang Kang, David T. Miller, Hong Shao, Qingwen Zhu, Jia He, Fei Yu, Xin Liu, Bing Han, Huijun Yuan, Orah S. Platt, Dongyi Han, Bai-Lin Wu	2008	51
7	Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation American Journal of Medical Genetics Part A ·Qiuju Wang, Roughua Li, Hui Zhao, Jennifer L. Peters, Qiong Liu, Li Yang, Dongyi Han, John H. Greinwald, Wie‐Yen Young, Min‐Xin Guan	2005	50
8	Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation Biochemical and Biophysical Research Communications ·Qiuju Wang, Qingzhong Li, Dongyi Han, Yali Zhao, Lidong Zhao, Yaping Qian, Yuan Hu, Ronghua Li, Suoqiang Zhai, Wie‐Yen Young, Min‐Xin Guan	2005	44
9	Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis Journal of Translational Medicine ·Pu Dai, Yongyi Yuan, Deliang Huang, Xiuhui Zhu, Fei Yu, Dongyang Kang, Huijun Yuan, Bai-Lin Wu, Dongyi Han, Lee‐Jun C. Wong	2008	44
10	Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness Biochemical and Biophysical Research Communications ·Pu Dai, Xin Liu, Dongyi Han, Yaping Qian, Deliang Huang, Huijun Yuan, Weiming Li, Fei Yu, Ruining Zhang, Hongyan Lin, Yong He, Youjun Yu, Quanzhu Sun, Huaiyi Qin, Ronghua Li, Xin Zhang, Dongyang Kang, Juyang Cao, Wie‐Yen Young, Min‐Xin Guan	2005	43
11	Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China Journal of Translational Medicine ·Feng Xin, Yongyi Yuan, Xiaoming Deng, Mingyu Han, Guojian Wang, Jiandong Zhao, Xue Gao, Jun Liu, Fei Yu, Dongyi Han, Pu Dai	2013	42
12	Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct Journal of Translational Medicine ·Shasha Huang, Dongyi Han, Yongyi Yuan, Guojian Wang, Dongyang Kang, Xin Zhang, Xiaofei Yan, Xiaoxiao Meng, Min Dong, Pu Dai	2011	38
13	Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNASer(UCN) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss Biochemical and Biophysical Research Communications ·Huijun Yuan, Jing Chen, Xin Liu, Jing Cheng, Xinjian Wang, Li Yang, Shuzhi Yang, Juyang Cao, Dongyang Kang, Pu Dai, Suoqiang Zhai, Dongyi Han, Wie‐Yen Young, Min‐Xin Guan	2007	35
14	Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation Mitochondrion ·Yuhua Zhu, Qi Li, Zheng‐Yi Chen, (unknown), Lijia Liu, Xin Liu, Huijun Yuan, Suoqiang Zhai, Dongyi Han, Pu Dai	2009	32
15	Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2 Journal of Translational Medicine ·Yongyi Yuan, Fei Yu, Guojian Wang, Shasha Huang, Ruili Yu, Xin Zhang, Deliang Huang, Dongyi Han, Pu Dai	2010	32
16	The mitochondrial tRNAAla T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss Biochemical and Biophysical Research Communications ·Dongyi Han, Pu Dai, Qingwen Zhu, Xin Liu, Deliang Huang, Yongyi Yuan, Huijun Yuan, Xinjian Wang, Yaping Qian, Wie‐Yen Young, Min‐Xin Guan	2007	32
17	Functional Mutation of SMAC/DIABLO, Encoding a Mitochondrial Proapoptotic Protein, Causes Human Progressive Hearing Loss DFNA64 The American Journal of Human Genetics ·Jing Cheng, Yuhua Zhu, Sudan He, Yanping Lu, Jing Chen, Bing Han, Marco Petrillo, Kazimierz O. Wrzeszczyński, Shiming Yang, Pu Dai, Suoqiang Zhai, Dongyi Han, Michael Q. Zhang, Wei Li, Xuezhong Liu, Huawei Li, Zheng Yi Chen, Huijun Yuan	2011	31
18	Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China Journal of Human Genetics ·Yi Sun, Jing Chen, Han-Jun Sun, Jing Cheng, Jianzhong Li, Yu Lu, Yanping Lu, Zhanguo Jin, Yuhua Zhu, Xiaomei Ouyang, Denise Yan, Pu Dai, Dongyi Han, Yang Wei–yan, Rongguang Wang, Xuezhong Liu, Huijun Yuan	2010	30
19	Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss Biochemical and Biophysical Research Communications ·Lidong Zhao, Qiuju Wang, Yaping Qian, Ronghua Li, Juayng Cao, Laura C. Hart, Suoqiang Zhai, Dongyi Han, Wie‐Yen Young, Min‐Xin Guan	2005	27
20	Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China PLoS ONE ·Yi Jiang, Shasha Huang, Tao Deng, Lihua Wu, Juan Chen, Dongyang Kang, Xiufeng Xu, Ruiyu Li, Dongyi Han, Pu Dai	2015	27

About Dongyi Han

Dongyi Han is a scholar working on Sensory Systems, Molecular Biology, Otorhinolaryngology, Neurology and Oncology, having authored 128 papers that have together received 1.8k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (68 papers), Ear Surgery and Otitis Media (20 papers), Vestibular and auditory disorders (16 papers), Mitochondrial Function and Pathology (15 papers), RNA and protein synthesis mechanisms (8 papers), Connexins and lens biology (7 papers), Ear and Head Tumors (6 papers) and Neuroscience of respiration and sleep (4 papers). The work is most often cited by research in Sensory Systems (1.1k citations), Otorhinolaryngology (231 citations), Neurology (339 citations), Clinical Biochemistry (88 citations) and Molecular Biology (874 citations). Dongyi Han has collaborated with scholars based in China, United States and Philippines. Frequent co-authors include Pu Dai, Huijun Yuan, Min‐Xin Guan, Yongyi Yuan, Dongyang Kang, Deliang Huang, Ronghua Li, Qiuju Wang, Wie‐Yen Young and Yidong Bai. Their work appears in journals such as Acta Oto-Laryngologica, Journal of Translational Medicine, PLoS ONE, Biochemical and Biophysical Research Communications and European Archives of Oto-Rhino-Laryngology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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Dongyi Han

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